Canonical Allele Identifier: CA2762037558
Gene: GNRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754499A>G , CM000666.2:g.67754499A>G GRCh38
NC_000004.11:g.68620217A>G , CM000666.1:g.68620217A>G GRCh37
NC_000004.10:g.68302812A>G NCBI36
NG_009293.1:g.6588T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-164T>C NP_000397.1:n.-164T>C
NM_001012763.1:c.-164T>C NP_001012781.1:n.-164T>C
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